Canonical Allele Identifier: CA675473
Gene: WNT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2283057
ClinVar RCV Id: RCV002840512 RCV003698992
dbSNP Id: rs377491760
ExAC: 1:22456127 C / T
gnomAD v2: 1-22456127-C-T
gnomAD v3: 1-22129634-C-T
gnomAD v4: 1-22129634-C-T
MyVariant Identifiers: chr1:g.22456127C>T (hg19) chr1:g.22129634C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129634C>T , CM000663.2:g.22129634C>T GRCh38
NC_000001.10:g.22456127C>T , CM000663.1:g.22456127C>T GRCh37
NC_000001.9:g.22328714C>T NCBI36
NG_008974.1:g.18393G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.295G>A MANE Select ENSP00000290167.5:p.Gly99Ser
ENST00000290167.10:c.295G>A ENSP00000290167.5:p.Gly99Ser
ENST00000415567.1:c.218G>A
ENST00000441048.1:c.130G>A ENSP00000388925.1:p.Gly44Ser
NM_030761.4:c.295G>A NP_110388.2:p.Gly99Ser
XM_011541597.1:c.361G>A XP_011539899.1:p.Gly121Ser
XM_011541598.1:c.130G>A XP_011539900.1:p.Gly44Ser
XM_011541599.1:c.361G>A XP_011539901.1:p.Gly121Ser
XM_011541597.2:c.361G>A XP_011539899.1:p.Gly121Ser
XM_011541598.2:c.130G>A XP_011539900.1:p.Gly44Ser
NM_030761.5:c.295G>A MANE Select NP_110388.2:p.Gly99Ser
Search 100 bp 5'
Search 100 bp 3'